[CMY-2-type plasmid-mediated AmpC ß-lactamases emerging in Tucumán, Argentina]

María A Jure1, Constanza Presti, Norma M Cudmani

  • 1Instituto de Microbiología Dr. Luis C. Verna, Cátedra de Bacteriología, Facultad de Bioquímica, Química, Farmacia y Biotecnología, Universidad Nacional de Tucumán, San Miguel de Tucumán. majure@fbqf.unt.edu.ar

Insights

This study detected CMY-2 type plasmid-mediated AmpC beta-lactamases in Enterobacteriaceae, highlighting the need for monitoring antimicrobial resistance to prevent clinical and epidemiological issues.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Clinical Science

Background:

  • Enterobacteriaceae, including Klebsiella pneumoniae, Proteus mirabilis, and Escherichia coli, are developing resistance to third-generation cephalosporins (C3G).
  • This resistance is primarily due to plasmid-mediated AmpC beta-lactamases.
  • The emergence of these resistant strains poses significant clinical and epidemiological challenges.

Purpose of the Study:

  • To detect and identify plasmid-mediated AmpC enzymes in Enterobacteriaceae isolates.
  • To investigate the predominant types of these enzymes in the region.
  • To understand the prevalence of antimicrobial resistance in local healthcare settings.

Main Methods:

  • Studied 733 Enterobacteriaceae isolates from March to July 2009.
  • Performed disk diffusion and E-test for antimicrobial susceptibility testing.
  • Utilized polymerase chain reaction (PCR) to detect specific ampC gene groups and sequence analysis.

Main Results:

  • Identified resistance to cephamycins and C3G in one P. mirabilis and three E. coli strains.
  • Confirmed enzymatic activity against cefoxitin.
  • PCR detected a 462-bp amplicon against the CIT group, with 100% sequence identity to blaCMY-2.

Conclusions:

  • CMY-2 type plasmid-mediated AmpC beta-lactamases are emerging in Enterobacteriaceae.
  • Systematic monitoring of these resistances is crucial.
  • Proactive surveillance can help mitigate potential clinical and epidemiological consequences of antimicrobial resistance.